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Peripheral neuropathy in chromosome16q22.1 linked autosomal dominant cerebellar ataxia. 2009

Yoshiko Furiya, and Makito Hirano, and Masami Nomura, and Hidehiro Asai, and Takao Kiriyama, and Satoshi Ueno
Nara Medical University, Neurology, Nara, 840 Shijo-cho, Kashihara-shi, Nara, 6348522, Japan.

Autosomal dominant cerebellar ataxia (ADCA) includes heterogeneous neurodegenerative diseases with or without various neurological signs and symptoms. Ishikawa et al reported a new type of ADCA, named chromosome16q22.1 linked ADCA (16q-ADCA), attributed to a heterozygous C→T substitution in the 5' non-coding region of puratrophin-1 gene. We searched for this mutation in168 patients from 129 families with ADCA and found it in six patients. The patients generally showed late onset pure cerebellar ataxia similar to previous reports but two had mild axonal neuropathy and orthostatic hypotension (OH). Our results suggest that 16q-ADCA shows a broader clinical presentation than previously thought.

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